Note : Les descriptions sont présentées dans la langue officielle dans laquelle elles ont été soumises.
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1 -5-HT2B RECEPTOR ANTAGONISTS
FIELD OF THE INVENTION
The present invention relates to novel fluorinated piperidine derivatives
having
antagonistic activity at the 5-HT2B receptor, pharmaceutical compositions
comprising
these compounds and their use as a medicine.
BACKGROUND OF THE INVENTION
Cisapride is a serotonin 5-HT4 receptor agonist useful as a gastroprokinetic
drug.
It interacts significantly with several other receptors such as 5-HT2A and 5-
HT2c; D2L.;
5-HT3A/B; AlphaiA, Alpha2A, Alpha2B and Alpha2c. It was withdrawn from some
markets in 2000 due to reports of sudden cardiac arrhythmias. At the origin of
this side
effect is drug-induced QT prolongation by blockade of the hERG potassium
channel
(human ether-a-go-go related gene). One of the known pharmacophores of a hERG
channel blocker comprises a hydrophilic and a hydrophobic moiety linked by a
middle
part having a basic nitrogen atom. At physiological pH, the basic nitrogen is
protonated
and is involved in cation-7c interaction with Tyr 652 residues within the hERG
channel
pore. In order to lower the pKa value of piperidine nitrogen atom, and thereby
reduce
the likelihood of blockade of the hERG channel, derivatives of cisapride were
prepared
wherein 3-methoxy-piperidine was replaced by 3-fluoropiperidine and 3,3-
difluoropiperidine.
SUMMARY OF THE INVENTION
The present invention concerns a compound of formula (I)
F
0 N N Cl
\ H
0 NH2
CH3
or a stereochemically isomeric form thereof, wherein
R is hydrogen or fluoro, or
an addition salt or a solvate thereof
Illustrative of the invention is a pharmaceutical composition comprising a
pharmaceutically acceptable carrier and any of the compounds described above.
An
illustration of the invention is a pharmaceutical composition made by mixing
any of the
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compounds described above and a pharmaceutically acceptable carrier.
Illustrating the
invention is a process for making a pharmaceutical composition comprising
mixing any
of the compounds described above and a pharmaceutically acceptable carrier.
Exemplifying the invention are methods of treating a disorder mediated by the
5-HT2B receptor, comprising administering to a subject in need thereof a
therapeutically
effective amount of any of the compounds or pharmaceutical compositions
described
above.
Further exemplifying the invention are methods of inhibiting the 5-HT2B
receptor, comprising administering to a subject in need thereof a
therapeutically
effective amount of any of the compounds or pharmaceutical compositions
described
above.
An example of the invention is a method of treating a disorder selected from
the
group consisting of pulmonary arterial hypertension, pulmonary fibrosis,
irritable
bowel syndrome, cardiovascular disorders such as chronic heart disease,
congestive
heart failure and hypertension, comprising administering to a subject in need
thereof, a
therapeutically effective amount of any of the compounds or pharmaceutical
compositions described above.
Another example of the invention is any of the compounds described above for
use in treating pulmonary arterial hypertension, pulmonary fibrosis, irritable
bowel
syndrome, cardiovascular disorders such as chronic heart disease, congestive
heart
failure and hypertension, in a subject in need thereof
DETAILED DESCRIPTION OF THE INVENTION
The present invention is directed to compounds of formula (I) as defined
hereinbefore, and pharmaceutically acceptable salts thereof The compounds of
formula
(I) are selective antagonists at the 5-HT2B receptor.
In an embodiment of the present invention, R is fluoro and the compound is a
racemic mixture or an addition salt or a solvate thereof
In another embodiment of the present invention, R is fluoro and the compound
has an optical rotation [a] = +14.10 (c=0.3, Me0H, = 598 nm; 20 C),
or an addition salt or a solvate thereof
In another embodiment of the present invention, R is fluoro and the compound
has an optical rotation [a] = -14.4 (c=0.3, Me0H, = 598 nm; 20 C),
or an addition salt or a solvate thereof
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In another embodiment of the present invention, R is hydrogen and the
substituents in position 3 and 4 of the piperidine moiety have a cis
orientation,
or an addition salt or a solvate thereof
In another embodiment of the present invention, R is hydrogen, the
substituents
in position 3 and 4 of the piperidine moiety have a cis orientation and the
compound
has an optical rotation [a] = +39.8 (c=0.2, Me0H, = 598 nm; 20 C),
or an addition salt or a solvate thereof
In another embodiment of the present invention, R is hydrogen, the
substituents
in position 3 and 4 of the piperidine moiety have a cis orientation and the
compound
has an optical rotation [a] = -45.5 (c=0.2, Me0H, = 598 nm; 20 C),
or an addition salt or a solvate thereof
In another embodiment of the present invention, R is hydrogen and the
substituents in position 3 and 4 of the piperidine moiety have a trans
orientation,
or an addition salt or a solvate thereof
In another embodiment of the present invention, R is hydrogen, the
substituents
in position 3 and 4 of the piperidine moiety have a trans orientation and the
compound
has an optical rotation [a] = +19.2 (c=0.4, Me0H, = 598 nm; 20 C),
or an addition salt or a solvate thereof
In another embodiment of the present invention, R is hydrogen, the
substituents
in position 3 and 4 of the piperidine moiety have a trans orientation and the
compound
has an optical rotation [a] = -22.8 (c=0.3, Me0H, = 598 nm; 20 C),
or an addition salt or a solvate thereof
As anticipated, the fluorinated cisapride derivatives are significantly less
potent
hERG channel blockers than cisapride and thus much less likely to cause drug-
induced
QT prolongation. Unexpectedly though, the receptor affinities change in
various ways
so as to yield compounds with a more selective profile. Affinities for 5-HT2A
and D2L
receptors diminish significantly, and for 5-HT3A/B, 5-HT4s, AlphaiA, Alpha2A,
Alpham
and Alpha2c receptors they show a trend to a reduction. The only exception is
the
affinity for the 5-HT2B receptor which increases significantly.
5-HT2B receptor antagonists are indicated for the treatment or the prevention
of
pulmonary arterial hypertension, pulmonary fibrosis or irritable bowel
syndrome.
Pulmonary arterial hypertension may be idiopathic, familial, or associated
with other
diseases such as HIV infection, or use of certain drugs. It may also be
associated with
heart or lung diseases such as chronic obstructive pulmonary disease (COPD),
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interstitial lung disease or chronic exposure to high altitude. Pulmonary
fibrosis is
characterized by chronic inflammation and progressive fibrosis of the alveolar
walls,
with steadily progressing dyspnea, resulting finally in death from oxygen lack
or right
heart failure. Irritable bowel syndrome is a chronic noninflammatory disease
characterized by abdominal pain, altered bowel habits consisting of diarrhea
or
constipation or both, and no pathological change. It is a common disorder with
a
psychophysiological basis. The 5-HT2B receptor antagonists may also be used to
treat
cardiovascular disorders such as chronic heart disease, congestive heart
failure and
hypertension.
DEFINITIONS
The term "subject" as used herein, refers to an animal, preferably a mammal,
most preferably a human, who is or has been the object of treatment,
observation or
experiment.
The term "therapeutically effective amount" as used herein, means that amount
of active compound or pharmaceutical agent that elicits the biological or
medicinal
response in a tissue system, animal or human that is being sought by a
researcher,
veterinarian, medical doctor or other clinician, which includes alleviation of
the
symptoms of the disease or disorder being treated.
As used herein, the term "composition" is intended to encompass a product
comprising the specified ingredients in the specified amounts, as well as any
product
which results, directly or indirectly, from combinations of the specified
ingredients in
the specified amounts.
It will be appreciated that some of the compounds according to formula (I) and
the addition salts, hydrates and solvates thereof may contain one or more
centers of
chirality and exist as stereoisomeric forms.
The term "stereoisomeric forms" as used hereinbefore or hereinafter defines
all
the possible stereoisomeric forms which the compounds according to formula (I)
and
their addition salts may possess. Unless otherwise mentioned or indicated, the
chemical designation of compounds denotes the mixture of all possible
stereochemically isomeric forms, said mixtures containing all diastereomers
and
enantiomers of the basic molecular structure as well as each of the individual
isomeric
forms according to formula (I) and their salts, solvates, substantially free,
i.e. associated
with less than 10%, preferably less than 5%, in particular less than 2% and
most
preferably less than 1% of the other isomers.
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Where the compounds according to this invention have at least one chiral
center, they may accordingly exist as enantiomers. Where the compounds possess
two
or more chiral centers, they may additionally exist as diastereomers. It is to
be
understood that all such isomers and mixtures thereof are encompassed within
the
scope of the present invention. Preferably, wherein the compound is present as
an
enantiomer, the enantiomer is present at an enantiomeric excess of greater
than or equal
to about 80%, more preferably, at an enantiomeric excess of greater than or
equal to
about 90%, more preferably still, at an enantiomeric excess of greater than or
equal to
about 95%, more preferably still, at an enantiomeric excess of greater than or
equal to
about 98%, most preferably, at an enantiomeric excess of greater than or equal
to about
99%. Similarly, wherein the compound is present as a diastereomer, the
diastereomer is
present at an diastereomeric excess of greater than or equal to about 80%,
more
preferably, at an diastereomeric excess of greater than or equal to about 90%,
more
preferably still, at an diastereomeric excess of greater than or equal to
about 95%, more
preferably still, at an diastereomeric excess of greater than or equal to
about 98%, most
preferably, at an diastereomeric excess of greater than or equal to about 99%.
Furthermore, some of the crystalline forms for the compounds of the present
invention may exist as polymorphs and as such are intended to be included in
the
present invention. In addition, some of the compounds of the present invention
may
form solvates with water (i.e., hydrates) or common organic solvents, and such
solvates
are also intended to be encompassed within the scope of this invention.
For use in medicine, the salts of the compounds of this invention refer to non-
toxic "pharmaceutically acceptable salts". Other salts may, however, be useful
in the
preparation of compounds according to this invention or of their
pharmaceutically
acceptable salts. Suitable pharmaceutically acceptable salts of the compounds
include
acid addition salts which may, for example, be formed by mixing a solution of
the
compound with a solution of a pharmaceutically acceptable acid such as
hydrochloric
acid, sulfuric acid, fumaric acid, maleic acid, succinic acid, acetic acid,
benzoic acid,
citric acid, tartaric acid, carbonic acid or phosphoric acid. Furthermore,
where the
compounds of the invention carry an acidic moiety, suitable pharmaceutically
acceptable salts thereof may include alkali metal salts, e.g., sodium or
potassium salts;
alkaline earth metal salts, e.g., calcium or magnesium salts; and salts formed
with
suitable organic ligands, e.g., quaternary ammonium salts.
Representative acids which may be used in the preparation of pharmaceutically
acceptable salts include, but are not limited to, the following: acetic acid,
2,2-dichloro-
acetic acid, acylated amino acids, adipic acid, alginic acid, ascorbic acid, L-
aspartic
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acid, benzenesulfonic acid, benzoic acid, 4- acetamidobenzoic acid, (+)-
camphoric
acid, camphorsulfonic acid, capric acid, caproic acid, caprylic acid, cinnamic
acid,
citric acid, cyclamic acid, ethane-1,2-disulfonic acid, ethanesulfonic acid, 2-
hydroxy-
ethanesulfonic acid, formic acid, fumaric acid, galactaric acid, gentisic
acid,
glucoheptonic acid, D-gluconic acid, D-glucoronic acid, L-glutamic acid, beta-
oxo-
glutaric acid, glycolic acid, hippuric acid, hydrobromic acid, hydrochloric
acid, (+)-L-
lactic acid, ( )-DL-lactic acid, lactobionic acid, maleic acid, (-)-L-malic
acid, malonic
acid, ( )-DL-mandelic acid, meglumine, methanesulfonic acid, naphthalene-2-
sulfonic
acid, naphthalene-1,5- disulfonic acid, 1-hydroxy-2-naphthoic acid, nicotinic
acid,
nitric acid, oleic acid, orotic acid, oxalic acid, palmitic acid, pamoic acid,
phosphoric
acid, L- pyroglutamic acid, salicylic acid, 4-amino-salicylic acid, sebacic
acid, stearic
acid, succinic acid, sulfuric acid, tannic acid, (+)-L-tartaric acid,
thiocyanic acid, p-
toluenesulfonic acid, trifluoromethylsulfonic acid, and undecylenic acid.
Some of the compounds according to formula (I) may also exist in their
tautomeric
form. Such forms although not explicitly indicated in the above formula are
intended
to be included within the scope of the present invention.
PHARMACEUTICAL COMPOSITIONS
The present invention also provides compositions for preventing or treating
diseases in which inhibition of pulmonary arterial hypertension or pulmonary
fibrosis is
beneficial.
Said compositions comprising a therapeutically effective amount of a
compound according to formula (I) and a pharmaceutically acceptable carrier or
diluent.
While it is possible for the active ingredient to be administered alone, it is
preferable to present it as a pharmaceutical composition. Accordingly, the
present
invention further provides a pharmaceutical composition comprising a compound
according to the present invention, together with a pharmaceutically
acceptable carrier
or diluent. The carrier or diluent must be "acceptable" in the sense of being
compatible
with the other ingredients of the composition and not deleterious to the
recipients
thereof
The pharmaceutical compositions of this invention may be prepared by any
methods well known in the art of pharmacy. A therapeutically effective amount
of the
particular compound, in base form or addition salt form, as the active
ingredient is
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combined in intimate admixture with a pharmaceutically acceptable carrier,
which may
take a wide variety of forms depending on the form of preparation desired for
administration. These pharmaceutical compositions are desirably in unitary
dosage
form suitable, preferably, for systemic administration such as oral,
percutaneous or
parenteral administration; or topical administration such as inhalation or
insufflation.
For example, in preparing the compositions in oral dosage form, any of the
usual
pharmaceutical media may be employed, such as, for example, water, glycols,
oils,
alcohols and the like in the case of oral liquid preparations such as
suspensions, syrups,
elixirs and solutions: or solid carriers such as starches, sugars, kaolin,
lubricants,
binders, disintegrating agents and the like in the case of powders, pills,
capsules and
tablets. Because of their ease in administration, tablets and capsules
represent the most
advantageous oral dosage unit form, in which case solid pharmaceutical
carriers are
obviously employed. For parenteral compositions, the carrier will usually
comprise
sterile water, at least in large part, though other ingredients, for example,
to aid
solubility, may be included. Injectable solutions, for example, may be
prepared in
which the carrier comprises saline solution, glucose solution or a mixture of
saline and
glucose solution. Injectable suspensions may also be prepared in which case
appropriate liquid carriers, suspending agents and the like may be employed.
In the
compositions suitable for percutaneous administration, the carrier optionally
comprises
a penetration enhancing agent and/or a suitable wettable agent, optionally
combined
with suitable additives of any nature in minor proportions, which additives do
not cause
any significant deleterious effects on the skin. Said additives may facilitate
the
administration to the skin and/or may be helpful for preparing the desired
compositions.
These compositions may be administered in various ways, e.g., as a transdermal
patch,
as a spot-on or as an ointment.
It is especially advantageous to formulate the aforementioned pharmaceutical
compositions in dosage unit form for ease of administration and uniformity of
dosage.
Dosage unit form as used in the specification and claims herein refers to
physically
discrete units suitable as unitary dosages, each unit containing a
predetermined quantity
of active ingredient calculated to produce the desired therapeutic effect in
association
with the required pharmaceutical carrier. Examples of such dosage unit forms
are
tablets (including scored or coated tablets), capsules, pills, powder packets,
suppositories, wafers, injectable solutions or suspensions, powders for
inhalation,
teaspoonfuls, tablespoonfuls and the like, and segregated multiples thereof
The exact dosage and frequency of administration depends on the particular
compound of formula (I) used, the particular condition being treated, the
severity of the
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condition being treated, the age, weight, sex, extent of disorder and general
physical
condition of the particular patient as well as other medication the individual
may be
taking, as is well known to those skilled in the art. Furthermore, it is
evident that said
effective daily amount may be lowered or increased depending on the response
of the
treated subject and/or depending on the evaluation of the physician
prescribing the
compounds of the instant invention.
Depending on the mode of administration, the pharmaceutical composition will
comprise from 0.05 to 99 % by weight, preferably from 0.1 to 70 % by weight,
more
preferably from 0.1 to 50 % by weight of the active ingredient, and, from 1 to
99.95 %
by weight, preferably from 30 to 99.9 % by weight, more preferably from 50 to
99.9 %
by weight of a pharmaceutically acceptable carrier, all percentages being
based on the
total weight of the composition.
The present compounds can be used for systemic administration such as oral,
percutaneous or parenteral administration; or topical administration such as
via
inhalation, a nose spray, eye drops or via a cream, gel, shampoo or the like.
The
compounds are preferably orally administered. The exact dosage and frequency
of
administration depends on the particular compound according to formula (I)
used, the
particular condition being treated, the severity of the condition being
treated, the age,
weight, sex, extent of disorder and general physical condition of the
particular patient
as well as other medication the individual may be taking, as is well known to
those
skilled in the art. Furthermore, it is evident that said effective daily
amount may be
lowered or increased depending on the response of the treated subject and/or
depending
on the evaluation of the physician prescribing the compounds of the instant
invention.
The amount of a compound of Formula (I) that can be combined with a carrier
material to produce a single dosage form will vary depending upon the disease
treated,
the mammalian species, and the particular mode of administration. However, as
a
general guide, suitable unit doses for the compounds of the present invention
can, for
example, preferably contain between 0.1 mg to about 1000 mg of the active
compound.
A preferred unit dose is between 1 mg to about 500 mg. A more preferred unit
dose is
between 1 mg to about 300 mg. Even more preferred unit dose is between 1 mg to
about 100 mg. Such unit doses can be administered more than once a day, for
example,
2, 3, 4, 5 or 6 times a day, but preferably 1 or 2 times per day, so that the
total dosage
for a 70 kg adult is in the range of 0.001 to about 15 mg per kg weight of
subject per
administration. A preferred dosage is 0.01 to about 1.5 mg per kg weight of
subject per
administration, and such therapy can extend for a number of weeks or months,
and in
some cases, years. It will be understood, however, that the specific dose
level for any
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particular patient will depend on a variety of factors including the activity
of the
specific compound employed; the age, body weight, general health, sex and diet
of the
individual being treated; the time and route of administration; the rate of
excretion;
other drugs that have previously been administered; and the severity of the
particular
disease undergoing therapy, as is well understood by those of skill in the
area.
A typical dosage can be one 1 mg to about 100 mg tablet or 1 mg to about 300
mg taken once a day, or, multiple times per day, or one time-release capsule
or tablet
taken once a day and containing a proportionally higher content of active
ingredient.
The time-release effect can be obtained by capsule materials that dissolve at
different
pH values, by capsules that release slowly by osmotic pressure, or by any
other known
means of controlled release.
It can be necessary to use dosages outside these ranges in some cases as will
be
apparent to those skilled in the art. Further, it is noted that the clinician
or treating
physician will know how and when to start, interrupt, adjust, or terminate
therapy in
conjunction with individual patient response.
The following examples are intended to illustrate but not to limit the scope
of the
present invention.
Experimental Part
Synthetic examples
Hereinafter, the term `m.p." means melting point, 'THY means tetrahydrofuran,
`DMF' means dimethylformamide, `DCM' means dichloromethane, 'Et0Ac' means
ethylacetate, "AcOH" means acetic acid, "Me0H" means methanol, "rac" means
racemic, "Et20" means diethylether, "DMAP" means dimethylaminopyridine,
"DMSO" means dimethylsulfoxide, "hex" means hexanes and "TFA" means
trifluoroacetic acid, DEA means diethylamine.
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Example 1 : Synthesis of trans-4-amino-5-chloro-N-{3-fluoro-1-[3-(4-
fluorophenoxy)-
bropyll-biperidin-4-y1}-2-methoxybenzamide 7.
0
a
Li-selectride
OH
N3
1) Et3N, TMSCIii
T
1) TosCI
2) Selectfluor
0HF C, 5h
CH2Cl2
2) NaN3
DMSO
Boo
Boo
Boo
Boc
1
2
3 (56%)
4 (92%)
Pd/C
HCOONH41,
,Boc ArCOOH
NH2
1) TFA, DCM, 0 C, 5h
OMe 0HOBt, EtCOOCI
2) Et3N, DMF, 110 C, 4h
Ns y
Et3N, DMF, it, 15h
,40 H2N
CI
6(93%)
Lc
(80%)
OMe 0
NO
chiral
(-9 7
[\11µsµY
separation
(-) 7
H2N
CI
7 (55%)
5
Synthesis of cis-1-Boc-3-fluoro-4-hydroxypiperidine 3
To a solution of 0.5 g (2.30 mmol) of N-Boc-3-fluoro-4-piperidinone 2 (J. Med.
Chem.
1999, 42, 2087-2104) in 10 mL of dry THF was added dropwise 2.8 mL (2.76 mmol)
of a 1M solution of Li-selectride in THF under N2-atmosphere at 0 C. The
solution was
stirred at 0 C for 4 h, then 10 mL of NaOH 2M was added at 0 C and the mixture
was
stirred overnight at rt. The reaction mixture was extracted with Et20, dried
over
Mg504, filtered and evaporated under reduced pressure. The crude mixture was
subjected to flash silicagel chromatography (hex/Et0Ac/Et3N 1:1:0.1) to yield
0.27 g
(56%) of pure cis-1-Boc-3-fluoro-4-hydroxypiperidine 3 as a colorless oil
which
solidified upon standing at -20 C (freezer). Mp 48 C. lEINMR (300 MHz, CDC13):
6
1.46 (9H, s, 3xCH3), 1.67-1.91 (2H, m, CH2), 2.40-2.65 (1H, m, OH), 2.92-3.35
(2H,
m, CH2CH,ElbN and CH,ElbCHF), 3.55-3.94 (3H, m, CH2CHaHhN and CHOH and
CHaHhCHF), 4.52 (1H, dm, J = 48.4 Hz, CHF). 19F NMR (282 MHz, CDC13): 6 -201.9
and -203.1 (1F, 2 x m). 13C NMR (75 MHz, CDC13): 6 28.4 (3x), 29.2, 40.4,
44.8, 68.0
(d, J = 17.3 Hz), 80.2, 88.6 (d, J = 177.7 Hz), 155.1. IR (KBr): v 3413, 1674,
1429,
1167 cm-1. GC-MS (EI): m/z (%): 219 (Mt, 4), 164 (46), 146 (50), 57 (C4H9t,
100).
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Synthesis of trans-4-azido-1-Boc-3-fluoropiperidine 4
To a solution of 0.60 g (2.74 mmol) of cis-1-Boc-3-fluoro-4-hydroxypiperidine
3 in 15
mL DCM was added 0.42 g (4.11 mmol) of triethylamine and 37 mg (0.3 mmol) of 4-
(N,N-dimethylamino)pyridine (DMAP) at rt. Then a solution of 0.57 g (3.01
mmol) of
p-toluenesulfonyl chloride in 2 mL of DCM was added under a dry atmosphere
(CaC12-
tube) at rt. After stirring for 15h at rt, the solution was poured in brine
(20 mL) and
extracted with DCM (3x 25 mL). After drying over Mg504, filtration and
evaporation
of the solvent, the crude mixture was used as such in the next step without
further
purification. The obtained tosylate was dissolved in 5 mL of dry DMSO and 0.36
g
(5.48 mmol) of NaN3 was added. The mixture was stirred under N2-atmosphere at
90 C
for 15h. After cooling, the mixture was poured in brine (10 mL) and extracted
with
Et0Ac. The combined extract were washed with brine, dried over Mg504, filtered
and
evaporated in vacuo. trans-4-Azido-1-Boc-3-fluoropiperidine 4 was obtained as
a
colorless oil in 92% yield from 4-hydroxypiperidine 3 and was sufficiently
pure for
further use. 1H NMR (CDC13): 6 1.43 (9H, s); 1.44-1.64(1H, m); 1.97 (1H, ddd,
J = 4.3
Hz, 8.4 Hz, 18.0 Hz); 2.99 (1H, ddd, J = 3.3 Hz, 10.5 Hz, 13.8 Hz); 3.00-3.15
(2H, m);
3.57-3.68 (1H, m); 3.79 (1H, dt, J = 13.8 Hz, J = 4.4 Hz); 4.00-4.19 (1H, m);
4.33 (tdd,
J = 47.9 Hz, J = 8.3 Hz, J = 4.4 Hz). 19F NMR (CDC13): 6 ¨188.1 (1F, d(br), J
= 47.4
Hz). 13C NMR (CDC13): 6 28.3 (4x), 41.2 (br), 45.5 (br), 61.4 (d, J = 20.7
Hz), 80.6,
88.9(d, J= 182.3 Hz), 154.4. IR (ATR, cm-1): v = 2099, 1693, 1417, 1236, 1161,
1141.
MS (ES+) m/z (%): 227 (M+H+, 100).
Synthesis of trans-4-amino-1-Boc-3-fluoropiperidine 5
To a solution of 0.59 g (2.42 mmol) of trans-4-azido-1-Boc-3-fluoropiperidine
4 in 10
mL of Me0H was added 0.61 g (9.67 mmol) of ammonium formate and 0.25 g (0.24
mmol Pd) of 10% Pd on carbon. The reaction mixture was stirred under N2-
atmosphere
at 50 C for 5h. After cooling, the mixture was filtered over diatomaceous
earth and
evaporated under reduced pressure. The crude mixture was then subjected to
flash
silicagel chromatography (5% Et3N in Et0Ac, short path column) to give 0.42 g
(80%)
of trans-4-amino-1-Boc-3-fluoropiperidine 5 as an oil. 1H NMR (CDC13): 6 1.39
(9H,
s); 1.60 (2H, s(br)); 1.76-1.86 (1H, m); 2.65-2.76 (2H, m); 2.78-2.90 (2H, m);
3.89-
3.97 (1H, m); 4.01 (1H, dm, J = 48.5 Hz); 4.15-4.30 (1H, m). 19F NMR (CDC13):
6 ¨
191.0 to -190.3 (1F, m). 13C NMR (CDC13): 6 28.4 (3x), 31.8, 41.9 (br), 46.2
(br), 53.5
(d, J = 18.5 Hz), 80.3, 93.0 (d, J = 177.7 Hz), 154.6. IR (ATR, cm-1): v =
1685, 1415,
1244, 1152, 1028. MS (ES+) m/z (%): 204 (M-CH3+H+), 163 (M-3CH3+2H+, 100).
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Synthesis of trans-tert-butyl 4-(4-amino-5-chloro-2-methoxybenzoylamino)-3-
fluoropiperidine-1-carboxylate 6
To a solution of 0.41 g (2.02 mmol) of 4-amino-5-chloro-2-methoxybenzoic acid
in 10
mL of dry DMF was added 0.29 g (2.89 mmol) of triethylamine at room
temperature
under N2-atmosphere. After stirring for 10 min at rt, a solution of 0.22 g
(2.02 mmol) of
ethyl chloroformate in 2 mL of DIVIF was added dropwise at rt and stirring was
continued for 30 min, while the temperature was maintained at rt (cooling with
waterbath at rt). Then 0.27 g (2.02 mmol) of hydroxybenzotriazole was added as
a solid
in one portion at rt and the solution was stirred for 30 min. Subsequently, a
solution of
0.42 g (1.93 mmol) of amine 5 in 3 mL of DIVIF was added dropwise at rt and
the
reaction mixture was stirred overnight at rt. Afterwards, the mixture was
poured in 20
mL of brine and extracted with Et0Ac (3x 25 mL). The combined organic fraction
was
washed with brine, dried over Mg504, filtered and evaporated under reduced
pressure.
The crude mixture was subjected to flash silicagel chromatography
(hex/Et0Ac/Et3N
1:1:0.1) to yield 0.72 g (93%) of pure trans-tert-butyl 4-(4-amino-5-chloro-2-
methoxybenzoylamino)-3-fluoropiperidine-1-carboxylate 6 as a solid. 1H NMR
(CDC13): 6 1.47 (9H, s); 2.17-2.28 (1H, m); 2.96-3.19 (2H, m); 3.74 (1H, dm, J
= 13.7
Hz); 3.90 (3H, s); 3.92-4.40 (3H, m); 4.45 (1H, ddt, J = 4.4 Hz, 8.3 Hz, J =
48.4 Hz);
6.30 (1H, s); 7.82 (1H, d, J = 7.2 Hz); 8.08 (1H, s). 19F NMR (CDC13): 6 -
189.0 (d, J =
44.7 Hz). 13C NMR (CDC13): 6 28.4 (3x), 29.1 (br), 41.5 (br), 45.6 (br), 50.1
(br), 56.4,
80.4, 88.2 (d, J= 182.3 Hz), 97.9, 111.8, 112.1, 133.2, 147.1, 154.7, 157.6;
164.5. IR
(ATR, cm-1): v = 3478, 3378, 1683, 1619, 1593, 1420, 1247, 1146. MS (ES+) m/z
(%):
346/48 (M+H+, 100); 402/404 (M+H+, 60).
Synthesis of trans-4-amino-5-chloro-N-{3-fluoro-1-[3-(4-fluorophenoxy)propyl]-
piperidin-4-y1}-2-methoxybenzamide 7.
To a solution of 0.14 g (0.34 mmol) of tert-butyl 4-(4-amino-5-chloro-2-
methoxybenzoylamino)-3-fluoropiperidine-1-carboxylate 6 in 5 mL of DCM was
added 0.39 g (3.4 mmol) of trifluoroacetic acid at 0 C under dry atmosphere
(CaC12-
tube). After stirring for 5 h at 0 C, the mixture was evaporated under reduced
pressure.
The oily residue was taken up in 10 mL of dry diethyl ether, cooled to 0 C and
the
formed crystalline TFA salt was isolated (filter or decant Et20). After drying
and
further evaporation the white crystalline TFA-salt of 4-amino-5-chloro-N-(3-
fluoropiperidin-4-y1)-2-methoxybenzamide was dissolved in 5 mL of dry DMF. To
the
solution was added 0.17 g (1.70 mmol) of triethylamine, 55 mg (0.34 mmol) of
sodium
iodide and then 65 mg (0.34 mmol) of 3-(4-fluorophenoxy)propy1-1-chloride at
rt under
dry atmosphere. The mixture heated to 110 to 120 C during 4h. After cooling,
the
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mixture was diluted with 25 mL of Et0Ac, poured in brine (25 mL) and extracted
with
Et0Ac (3x 25 mL). The combined organic phase was washed with brine, dried over
MgSO4, filtered and evaporated under reduced pressure. The crude mixture was
subjected to gradient flash silicagel chromatography (Et0Ac/hex/Et3N 3:2:0.1
to 1%
Et3N in Et0Ac) to give 85 mg (55%) of trans-4-amino-5-chloro-N-{3-fluoro-1-[3-
(4-
fluorophenoxy)propyl]piperidin-4-y1}-2-methoxybenzamide 7 as a pale yellow
solid.
Mp 125 C. Optional recrystallization from Et0Ac/Et0H.1EINMR (CDC13): 6 1.46-
1.59 (1H, m); 1.94 (2H, quint, J = 6.6 Hz); 2.18-2.34 (3H, m); 2.58 (2H, t, J
= 6.6 Hz);
2.76 (1H, dm, J = 11.6 Hz); 3.13 (1H, td(br), J = 4.4 Hz, 9.9 Hz); 3.87 (3H,
s); 3.96
(2H, t, J = 6.6 Hz); 4.09-4.23 (1H, m); 4.47 (1H, ddt, J = 4.4 Hz, J = 9.4 Hz,
J = 49.5
Hz); 4.48 (2H, s(br)); 6.02 (1H, s); 6.79-6.86 (2H, m); 6.92-7.00 (2H, m);
7.79 (1H, d, J
= 7.7 Hz), 8.09 (1H, s). 19F NMR (CDC13): 6 ¨187.6 (d, J = 51.3 Hz); -124.0
(tt, J = 3.9
Hz, J = 9.2 Hz). 13C NMR (CDC13): 6 27.0, 29.9 (d, J = 6.9 Hz), 51.0 (d, J =
18.5 Hz),
51.5, 54.6, 56.2, 56.3 (d, J = 24.2 Hz), 66.7, 89.0, 90.2(d, J = 178.8 Hz),
97.9, 111.7,
112.3, 2 x 115.5 (d, J = 8.0 Hz), 2 x 115.8 (d, J = 23.0 Hz), 133.2, 147.0,
155.2, 157.3
(d, J = 238.9 Hz), 157.6, 164.6. IR (ATR, cm-1): v = 3453, 3370, 3317, 3194,
1631,
1584, 1537, 1508, 1250, 1200. MS (ES+) m/z (%): 454/456 (M+H+, 100).
Chiral separation of trans-4-amino-5-chloro-N-{3-fluoro-1-[3-(4-fluorophenoxy)-
propyll-piperidin-4-y1}-2-methoxybenzamide 7.
Compound 7 was resolved into its enantiomers by supercritical fluid
chromatography.
Amount: 80 mg (Load: 10 mg/ 3.00 ml)
Conditions:
Column: OD 20x250mm (I)
Mobile Phase: 37% Me0H (with 0.2% iPrNH2) hold 9.00 min
Parameters: Flow =50 ml/min
Column temperature =40 C
Nozzle pressure = 10 MPa
Injection type: stacked injections (8 x)
Collection method: Collection using standard peak detection.
Peak 1 eluted at 5 min 20' and yielded the levorotatory enantiomer (-)-7
[a] = -22.8 (c=0.3, Me0H, = 598 nm; 20 C).
Peak 2 eluted at 7 min 30' and yielded the dextrorotatory enantiomer (+)-7
[a] = +19.2 (c=0.4, Me0H, = 598 nm; 20 C).
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Example 2: Synthesis of cis-4-amino-5-chloro-N-{3-fluoro-143-(4-fluorophenoxy)-
propyll-piperidin-4-y1}-2-methoxybenzamide 12.
0 1) Et3N, TMSCI BnNH2 Bn NH NH4OCHO
2) Selectfluor Na(0Ac)3BH Pd/C, Me0H
(Lit. ref 1) (Lit. ref 2) (Lit. ref 2)
Bac Bac Bac
1 8 9(63%)
NH2
B o c ArCOOH p I -
1) TFA, DCM, 0 C, 4h OMe 0 N HOBt, EtCOOCI
2) Et3N, DMF, 120 C, 2h Et3N, DMF, it, 15h
H F Bac
CI H2N CI 11(68%) 10 (95%)
OMe 0 0' chiral (+)-12
H2N 11 F separation (-)-12
CI 12(49%)
Synthesis of cis-N-(1-B oc-3-fluoropiperidin-4-yl)amine 10
The compound was prepared as disclosed in literature references:
1)1 Med. Chem. 1999, 42, 2087-2104, and
2) WO 2007071965.
Synthesis of cis-tert-butyl 4-(4-amino-5-chloro-2-methoxybenzoylamino)-3-
fluoro-
piperidine-1-carboxylate 11
To a solution of 0.97 g (4.82 mmol) of 4-amino-5-chloro-2-methoxybenzoic acid
in 25
mL of dry DMF was added 0.70 g (6.88 mmol) of triethylamine at room
temperature
under N2-atmosphere. After stirring for 10 min at rt, a solution of 0.52 g
(4.82 mmol) of
ethyl chloroformate in 1 mL of DMF was added dropwise at rt and stirring was
continued for 30 min. Then 0.65 g (4.82 mmol) of hydroxybenzotriazole was
added as
a solid in one portion at rt and the solution was stirred for 30 min.
Subsequently, a
solution of 1.0 g (4.59 mmol) of amine 10 in 3 mL of DMF was added dropwise at
rt
and the reaction mixture was stirred overnight at rt. Afterwards, the mixture
was poured
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in 100 mL of brine and extracted with Et0Ac (4x 30 mL). The combined organic
fraction was washed with brine, dried over MgSO4, filtered and evaporated
under
reduced pressure. The crude mixture was subjected to flash silicagel
chromatography
(hex/Et0Ac/Et3N 1:1:0.1; Rf = 0.01) to yield 1.25 g (68%) of pure tert-butyl 4-
(4-
amino-5-chloro-2-methoxybenzoylamino)-3-fluoropiperidine-l-carboxylate 11 as a
solid. Mp 198-199 C.114NMR (CDC13): 6 1.35 (9H, s); 1.44-1.77 (2H, m); 2.77-
2.98
(1H, m); 3.81 (3H, s); 4.04-4.32 (4H, m); 4.42 (2H, s(br)); 4.65 (1H, d, J =
48.9 Hz);
6.23 (1H, s); 7.95 (1H, s(br)); 8.01 (1H, s). 19F NMR (CDC13): 6 ¨203.5 to -
204.5 (1F,
m). 13C NMR (CDC13): 6 26.6, 28.5 (3x), 42.3 (br), 46.5 (br), 48.6 (d, J =
17.3 Hz),
52.2, 80.1, 87.9 (d, J = 176.5 Hz), 97.9, 111.6, 112.0, 133.1, 147.1, 155.2,
157.7, 164Ø
IR (ATR, cm-1): v = 3470, 3393, 3310, 1697, 1637, 1612, 1534, 1420. MS (ES+)
m/z
(%): 402/404 (M+H+, 100).
Synthesis of cis-4-amino-5-chloro-N-{3-fluoro-1-[3-(4-fluorophenoxy)propyl]-
piperidin-4-y1}-2-methoxybenzamide 12.
To a solution of 1.00 g (2.49 mmol) of tert-butyl 4-(4-amino-5-chloro-2-
methoxybenzoylamino)-3-fluoropiperidine-1-carboxylate 11 in 10 mL of DCM was
added 2.83 g (24.9 mmol) of trifluoroacetic acid at 0 C under dry atmosphere
(CaC12-
tube). After stirring for 4 h at 0 C, the mixture was evaporated under reduced
pressure.
The oily residue was taken up in 25 mL of dry diethyl ether, cooled to 0 C and
the
formed crystalline TFA salt was isolated (filter or decant Et20). After drying
and
further evaporation in vacuo 0.78 g of the TFA-salt of 4-amino-5-chloro-N-(3-
fluoropiperidin-4-y1)-2-methoxybenzamide was obtained as a white solid. To a
solution
of 0.78 g of the obtained salt in 10 mL of DMF was added 1.26 g (12.45 mmol)
of
triethyl amine, 0.37 g (2.49 mmol) of sodium iodide and then 0.47 g (2.49
mmol) of 3-
(4-fluorophenoxy)propy1-1-chloride at rt under dry atmosphere. The mixture
heated to
120 C for 2h. After cooling, the mixture was diluted with 25 mL of Et0Ac,
poured in
brine (25 mL) and extracted with Et0Ac (3x 25 mL). The combined organic phase
was
washed with brine, dried over Mg504, filtered and evaporated under reduced
pressure.
The crude mixture was subjected to gradient flash silicagel chromatography
(Et0Ac/hex/Et3N 3:1:0.1 to 1% Et3N in Et0Ac) to give 49% of 4-amino-5-chloro-N-
{3-fluoro-143-(4-fluorophenoxy)propyl]piperidin-4-y1}-2-methoxybenzamide 12 as
a
pale yellow solid. Mp 137 C. Optional recrystallization from Et0Ac/Et0H.11-1
NIVIR
(CDC13): 6 1.83-1.92 (2H, m); 1.94 (2H, quint, J = 6.6 Hz); 2.10-2.35 (2H, m);
2.47-
2.61 (2H, m); 2.94 (1H, d(br), J= 11.6 Hz); 3.24 (1H, t(br), J= 11.3 Hz); 3.85
(3H, s);
3.95 (2H, t, J = 6.6 Hz); 4.08-4.27 (1H, m); 4.41 (2H, s(br)); 4.73 (1H,
d(br), J = 49.6
Hz); 6.26 (1H, s), 6.76-6.84 (2H, m); 6.89-6.97 (2H, m); 8.03 (1H, s(br));
8.06 (1H, s).
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19F NMR (CDC13): 6 ¨199.3 to -200.0 (1F, m); -124.1 (1F, tt, J = 7.9 Hz, J =
5.3 Hz).
13C NMit (CDC13): 6 26.9, 27.4, 48.3 (d, J = 18.4 Hz), 52.0, 54.7, 56.1 (d, J=
18.3 Hz),
56.2, 66.8, 88.8 (d, J = 175.3 Hz), 97.9 Hz, 111.6, 112.2,2 x 115.6 (d, J =
8.0 Hz), 2 x
115.8 (d, J = 23.1 Hz), 133.1, 147.0, 155.2, 157.2 (d, J = 237.7 Hz), 157.7,
164Ø IR
(ATR, cm-1): v = 3477, 3398, 3322, 1636, 1612, 1583, 1537, 1505, 1247, 1209.
MS
(ES+) m/z (%): 454/456 (M+H+, 100).
Chiral separation of cis-4-amino-5-chloro-N-{3-fluoro-1-[3-(4-
fluorophenoxy)propy1]-
piperidin-4-y1}-2-methoxybenzamide 12.
Compound 12 was resolved into its enantiomers by supercritical fluid
chromatography.
Amount: 152 mg (Load: 8.5 mg/ 1.250 ml)
Conditions:
Column: OJ 20x250mm (I)
Mobile Phase: 19% Me0H (with 0.2% iPrNH2) hold 14.00 min
Parameters: Flow = 50 ml/min
Column temperature =40 C
Nozzle pressure = 10 MPa
Injection type: stacked injections (18 x)
Collection method: Collection using standard peak detection.
Peak 1 eluted at 10 min 20' and yielded the levorotatory enantiomer (-)-12
[a] = -45.5 (c=0.2, Me0H, = 598 nm; 20 C).
Peak 2 eluted at 11 min 40' and yielded the dextrorotatory enantiomer (+)-12
[a] = +39.8 (c=0.2, Me0H, = 598 nm; 20 C).
Example 3 : Synthesis of 4-amino-5-chloro-N-{3,3-difluoro-143-(4-
fluorophenoxy)-
propyll-piperidin-4-y1}-2-methoxybenzamide 17
Synthesis of benzyl-(3,3-difluoro-piperidin-4-yl)amine 14
In a 100 mL flask, 2.00 g (8.0 mmol) of 3,3-difluoro-4,4-dihydroxy-1-
trifluoroacetylpiperidine 13 (J. Org Chem. 2010, 75, 929-932) and 2.15 g (20.0
mmol;
2.5 equiv) of benzylamine were dissolved in 50 mL of toluene. The mixture was
heated
under reflux with a Dean Stark trap during 15 hours. After cooling to room
temperature, the solvent was removed in vacuo. The resulting oil was dissolved
in 25
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mL of absolute methanol and 0.56 g (8.8 mmol; 1.1 equiv) of sodium
cyanoborohydride and 0.48 g (8.0 mmol; 1 equiv) of acetic acid were slowly
added at
room temperature. The solution was stirred during 4 hours at room temperature.
After
removing the solvent under vacuum, the crude oil was redissolved in 50 mL of
dichloromethane and poured in 50 mL of a saturated aqueous NaHCO3 solution and
was subsequently extracted with dichloromethane (3 x 50 mL). The combined
organic
layers were washed with brine and dried over MgSO4. Filtration of the solids
and
evaporation of the solvent resulted in a crude oil which was purified via
flash
chromatography (Et0Ac, Rf = 0.03) yielding 1.32 g (5.8 mmol; 73% yield) of
benzyl-
(3,3-difluoro-piperidin-4-yl)amine 14 as a yellow oil.
1E1 NMR (CDC13): 6 1.51 (1H, q, J= 11.8 Hz, CHaElb); 1.69 (1H, s(broad), NH);
1.94
(1H, d, J = 11.8 Hz, CHallb); 2.58 (1H, t, J = 12.8 Hz, NCHaElb); 2.74 (1H,
dd, J = 25.3
Hz, 14.3 Hz, NCHaHbCF2); 2.86-2.97 (1H, m, NCH); 3.02 (1H, d, J = 12.8 Hz,
NCHallb); 3.22 (1H, dt, J = 14.3 Hz, 9.4 Hz, NCHallbCF2); 3.91 (1H, d, J =
14.9 Hz,
CHafIbPh); 3.96 (1H, d, 14.9 Hz, CHaa,Ph); 7.22-7.38 (5H, m, 5 x CHar). 19F
NMR
(CDC13): 6 -109.0 (1F, d, J = 234.1 Hz); -120.4 (1F, d(broad), J = 234.1 Hz).
13C NMR
(CDC13): 6 31.9 (CH2); 43.3 (NCH2); 50.5 (t, J = 27.1 Hz, NCH2CF2); 51.5
(NCH2Ph);
57.1 (t, J = 20.8 Hz, NCH); 120.9 (t, J = 247.5 Hz, CF2); 126.9 (CHar); 127.9
(2 x
CHar); 128.3 (2 x CHar); 140.1 (Car). IR (ATR, cm-1): v = 3324 (NH); 3028;
2930;
2859; 1495; 1453; 1317; 1274; 1181; 1130; 1106; 1072; 983; 912; 855; 740; 699.
MS
(ES+) m/z (%): 227 (M+H+, 100).
Synthesis of benzyl-{3,3-difluoro-143-(4-fluoro-phenoxy)propyl]piperidin-4-
ylIamine
25 In a 100 mL flask, a mixture of 1.22 g (5.4 mmol) of benzyl-(3,3-difluoro-
piperidin-4-
yl)amine 14, 0.81 g (5.4 mmol; 1 equiv) of sodium iodide, 2.73 g (27.0 mmol; 5
equiv)
of triethylamine and 1.05 g (5.4 mmol; 1 equiv) of 1-(3-chloropropoxy)-4-
fluorobenzene in 70 mL was stirred at 120 C during 30 hours. Another portion
of 2.73
g (27.0 mmol; 5 equiv) of triethylamine was added and the mixture stirred at
120 C
30 during 16 hours. Then 1.05 g (5.4 mmol; 1 equiv) of 1-(3-chloropropoxy)-4-
fluorobenzene was added and the mixture was stirred at 120 C during 54 hours
until
the reaction was completed. The solvent was removed under vacuum and the crude
oil
was redissolved in 100 mL of Et0Ac and washed with brine and dried over Mg504.
Filtration of the solids and evaporation of the solvent resulted in a crude
oil which was
35 purified via flash chromatography (hexane/Et0Ac 1:1, Rf = 0.19-0.38)
yielding 1.00 g
(2.6 mmol; 49% yield) of benzyl-{3,3-difluoro-143-(4-fluoro-
phenoxy)propyl]piperidin-4-ylIamine 15 as a brown oil.
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1H NMR (CDC13): 6 1.48-1.62 (1H, m, CHaHb); 1.58 (1H, s(broad), NH); 1.80-1.92
(1H, m, CHallb); 1.86 (2H, quintet, J = 6.9 Hz, CH2); 2.09 (1H, t, J = 10.7
Hz,
NCHaHb); 2.26 (1H, ddd, J = 23.8 Hz, 12.3 Hz, 3.4 Hz, NCHaHbCF2); 2.41-2.57
(2H,
m, NCH2); 2.68-2.82 (2H, m, NCH and NCHallb); 2.99 (1H, td, J = 11.3 Hz, 8.8
Hz,
NCHallbCF2); 3.84 (1H, d, J = 14.0 Hz, CHaHbP11); 3.89 (2H, t, J = 6.9 Hz,
OCH2);
3.91 (1H, d, 14.0 Hz, CHallbP11); 6.74 (2H, dd, J = 9.4 Hz, 4.4 Hz, 2 x CHar);
6.87 (2H,
t, J = 9.4 Hz, 2 x CHar); 7.14-7.30 (5H, m, 5 x CHar). 19F NMR (CDC13): 6 -
104.9 (IF,
d, J = 225.6 Hz, CF b); -116.9 (IF, d(broad), J = 225.6 Hz, CFaEb); -124.0
(IF, tt, J =
7.9 Hz, 4.0 Hz, Ca,F). 13C NMR (CDC13): 6 26.7 (CH2, alkyl); 29.2 (d, J = 5.8
Hz, CH2);
50.8 (NCH2); 51.5 (NCH2Ph); 53.9 (NCH2, alkyl); 57.0 (t, J = 20.8 Hz, NCH);
57.2 (t, J
= 27.7 Hz, NCH2CF2); 66.4 (OCH2); 115.4 (d, J = 8.1 Hz, 2 x CHar); 115.7 (d, J
= 23.1
Hz, 2 x CHar); 120.9 (t, J = 245.2 Hz, CF2); 127.0 (CHar); 128.0 (2 x CHar);
128.5 (2 x
CHar); 140.2 (Car); 155.0 (d, J = 2.3 Hz, OCar); 157.1 (d, J = 238.8 Hz,
Ca,F). IR (ATR,
cm-1): v = 3334 (NH); 3062; 3028; 2953; 2823; 1682; 1602; 1505; 1470; 1454;
1388;
1346; 1292; 1247; 1205; 1152; 1118; 1097; 1064; 1028; 987; 912; 828; 736; 699.
MS
(ES+) nilz (%): 379 (M+H+, 100).
0CF3 1) 2.5 equiv BflNH2
2
equiv Nal
toluene, A, 15 h H
10 equiv Et3N
(Dean Stark)
2 equiv R-CI
F
\/\ F 2) 1.1 equiv NaCNBH3
F DMF, 120 C, 100
h
F
HOOH F /\ 1 equiv AcOH
NH F
NH
F
Me0H, rt, 4 h
13
14 (73%)
15 (49%)
40% Pd/C
H2 (480 kPa)
Me0H, it, 15 h
1.05 equiv
H2N OMe
(+)-17 separation chiral 0 NH
F F
CI COOH
F F F
(-)-17
1.5 equiv Et3N
NH2
1.05 equiv EtOCOCI
1.05 equiv HOBt
16 (90%)
CI DMF, it, 15 h
NH2
17(71%)
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Synthesis of 3,3-difluoro-1-[3-(4-fluorophenoxy)propyl]piperidin-4-amine 16
In a dry pressure vessel, 0.83 g (2.2 mmol) of benzyl-{3,3-difluoro-143-(4-
fluoro-
phenoxy)propyl]piperidin-4-ylIamine 15 was dissolved in 10 mL of methanol.
After
adding 0.33 g (40wt%) of Pd/C (10%) at 0 C, the mixture was stirred during 15
hours
at room temperature under hydrogen pressure of 480 kPa. The mixture was
filtered
over diatomaceous earth. The solvent was evaporated in vacuo to yield 0.57 g
(2.0
mmol; 90% yield) of 3,3-difluoro-143-(4-fluorophenoxy)propyl]piperidin-4-amine
16
as a yellow oil.
1E1 NMR (CDC13): 6 1.54 (1H, dddd, J = 24.5 Hz, 11.3 Hz, 3.7 Hz, 1.7 Hz,
CHaElb);
1.80-1.99 (1H, m, CHallb); 1.86 (2H, quintet, J = 6.7 Hz, CH2); 2.11 (1H, t, J
= 11.6
Hz, NCHaHb); 2.21 (1H, ddd, J = 26.4 Hz, 12.1 Hz, 2.2 Hz, NCHaHbCF2); 1.42
(2H,
s(broad), NH2); 2.44-2.61 (2H, m, NCH2); 2.76-2.92 (2H, m, NCH and NCHallb);
3.00-
3.13 (1H, m, NCHallbCF2); 3.90 (2H, t, J = 6.7 Hz, OCH2); 6.75 (2H, dd, J =
9.4 Hz,
4.4 Hz, 2 x CHar); 6.88 (2H, t, J = 9.4 Hz, 2 x CHar). 19F NMR (CDC13): 6 -
109.6 (1F,
d, J = 239.4 Hz, CF b); -120.5 (1F, d(broad), J = 239.4 Hz, CFaEb); -124.0
(1F, tt, J =
7.9 Hz, 4.0 Hz, Ca,F). 13C NMR (CDC13): 6 26.8 (CH2, alkyl); 30.6 (d, J = 6.9
Hz, CH2);
51.4 (NCH2); 52.8 (t, J = 22.5 Hz, NCH); 53.9 (NCH2, alkyl); 57.0 (dd, J =
29.4 Hz, 24.8
Hz, NCH2CF2); 66.4 (OCH2); 115.4 (d, J = 6.9 Hz, 2 x CHar); 115.7 (d, J = 21.9
Hz, 2
x CHar); 119.6 (dd, J = 245.8 Hz, 241.1 Hz, CF2); 155.0 (0Car); 157.2 (d, J =
237.7 Hz,
Ca,F). IR (ATR, cm-1): v = 3384; 2952; 2821; 1601; 1505; 1470; 1390; 1348;
1294;
1247; 1204; 1146; 1078; 915; 828; 757; 735. MS (ES+) m/z (%): 289 (M+H+, 100).
Synthesis of 4-amino-5-chloro-N-{3,3-difluoro-1-[3-(4-fluorophenoxy)propy1]-
piperidin-4-y1}-2-methoxybenzamide 17
In a dry 50 mL flask, 0.44 g (2.2 mmol; 1.1 equiv) of 4-amino-5-chloro-2-
methoxybenzoic acid and 0.30 g (3 mmol; 1.5 equiv) of triethylamine were
dissolved in
25 mL of dimethylformamide and stirred during 10 minutes at room temperature.
Then
the mixture was cooled to 0 C and 0.24 g (2.2 mmol; 1.1 equiv) of ethyl
chloroformate
was added and stirred during 30 minutes at room temperature. Then 0.29 g (2.2
mmol;
1.1 equiv) of 1-hydroxybenzotriazole was added and stirred during 30 minutes
at room
temperature. Then 0.57 g of 3,3-difluoro-143-(4-fluorophenoxy)propyl]piperidin-
4-
amine 16 was added and the mixture was stirred at room temperature during 15
hours.
After evaporation of the solvent in vacuo, the crude oil was redissolved in
Et0Ac and
poured in 50 mL of brine and extracted with Et0Ac (4 x 50 mL). The organic
phases
were washed with brine and dried over Mg504. After filtration of the solids
and
evaporation of the solvent under vacuum, the crude oil was purified via flash
chromatography (hexane/Et0Ac 3:7, Rf = 0.35) yielding 0.66 g (1.4 mmol; 71%
yield)
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of pure 4-amino-5-chloro-N-{3,3-difluoro-143-(4-fluorophenoxy)propyl]piperidin-
4-
y1I-2-methoxybenzamide 17 as white crystals. M.p. = 125.8 C (hexane/Et0H
1:1).
1H NMR (CDC13): 6 1.70 (1H, ddd, J = 24.8 Hz, 12.7 Hz, 3.9 Hz, CHaElb); 1.93
(2H,
quintet, J = 6.6 Hz, CH2); 2.01-2.12 (1H, m, CHallb); 2.21 (1H, t, J = 11.8
Hz,
NCHaElb); 2.34 (1H, ddd, J = 28.8 Hz, 11.3 Hz, 1.7 Hz, NCHaHbCF2); 2.50-2.69
(2H,
m, NCH2); 2.92 (1H, d, J = 11.8 Hz, NCHallb); 3.19 (1H, td, J = 11.3 Hz, 4.4
Hz,
NCHallbCF2); 3.86 (3H, s, OCE13); 3.96 (2H, t, J = 6.6 Hz, OCH2); 4.43 (3H,
s(broad),
NCH and NH2); 6.26 (1H, s, CHar); 6.81 (2H, dd, J = 8.8 Hz, 4.4 Hz, 2 x CHar);
6.94
(2H, t, J = 8.8 Hz, 2 x CHar); 8.03 (1H, s(broad), NH); 8.06 (1H, s, CHar).
19F NMR
(CDC13): 6 -107.6 (1F, d, J = 240.7 Hz, CF b); -116.9 (1F, d(broad), J = 240.7
Hz,
CFaFb); -124.0 (1F, tt, J = 7.9 Hz, 4.0 Hz, CarF). 13C NMR (CDC13): 6 26.8
(CH2, alkyl);
29.6 (d, J = 5.8 Hz, CH2); 50.2 (t, J = 19.6 Hz, NCH); 51.5 (NCH2); 53.9
(NCH2, alkyl);
56.2 (OCE13); 58.0 (dd, J = 29.4 Hz, 23.7 Hz, NCH2CF2); 66.3 (OCH2); 97.8
(CHar);
111.6 (carC0); 111.9 (CarC1); 115.4 (d, J = 8.1 Hz, 2 x CHar); 115.7 (d, J =
23.1 Hz, 2 x
CHar); 118.9 (t, J = 245.8 Hz, CF2); 133.1 (CHar); 147.1 (CarNH2); 155.0 (d, J
= 2.3 Hz,
OCar); 157.2 (d, J = 237.7 Hz, CarF); 157.6 (carOMe); 164.4 (C=0). IR (ATR, cm-
1): v
= 3480; 3398; 3329; 3194; 2964; 2886; 2818; 1641; 1614; 1584; 1538; 1506;
1462;
1318; 1247; 1208; 1146; 1124; 1074; 1037; 982; 910; 822; 753; 681. MS (ES+)
m/z
(%): 472/474 (M+H+, 100).
Chiral separation of 4-amino-5-chloro-N-{3,3-difluoro-1-[3-(4-
fluorophenoxy)propy1]-
piperidin-4-y1}-2-methoxybenzamide 17
170 mg of 17 was resolved into its enantiomers by supercritical fluid
chromatography
on a Berger MultigramTM SFC (Mettler, Toledo Co., Ltd) with an IC 250 mm*50mm,
5mm column.
Mobile phase : supercritical CO2 : Me0H with 0.05% DEA = 75:25 at 160 ml/min
Column temperature : 38 C
Nozzle pressure: 30 NiPa
Nozzle temperature: 60 C
Evaporator temperature : 20 C
Trimmer temperature : 25 C
Wavelength: 220 nm.
Peak 1 eluted at 7.4 min and yielded the dextrorotatory enantiomer (+)-17
e.e.% = 100%; [a] = +14.1 (c=0.3, Me0H, = 598 nm; 20 C).
Peak 2 eluted at 8.5 min and yielded the levorotatory enantiomer (-)-17
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e.e.% = 98.6 %; [a] = -14.4 (c=0.3, Me0H, = 598 nm; 20 C).
Pharmacological examples
Example 4 : Receptor binding
Competitive radioligand binding assays were used to determine the affinity of
the test
compounds for a particular receptor. Various concentrations of the non-
labelled test
compound were added to the incubation mixture with the membrane fraction,
containing the receptor of interest, and a fixed low concentration (nM) of the
radioligand. During the incubation the radioligand bound to the receptor, but
this was
inhibited by the non-labelled test compound in proportion to its binding
affinity and
concentration.
Cell lines were established that stably express the human variant of the
receptor under
investigation after transfection with the appropriate cDNA (Table 1).
Transfected cells
were grown under standard culture conditions, and membrane fractions were
obtained
upon centrifugation and homogenisation of the cells. Optimal membrane
dilutions for
binding studies were determined and aliquots were stored at -70 C until use.
In a 96-
well plate format, the appropriate radioligand was added to the membrane
preparation
containing the receptor under investigation. Compound solutions were prepared
in
DMSO, and diluted 100-fold into the multiwell plate to a final test
concentration of
10-9 to 10-5 M. After incubation with the test compound, the unbound
radioligand was
removed by filtration on G/F filters with a Filtermate 96. MicroscintTM was
added to
the washed filter plates and the radioactivity bound to the receptor was
measured by
liquid scintillation counting in a TopCount (Packard). To measure the Non-
Specific
Binding (NSB), a high concentration of the non-radiolabeled ligand was added
to wells
containing the membrane fraction and the radioligand.
Table 1: Summary of assay conditions for inhibition of radioligand binding to
the
receptors evaluated.
Receptor Cell line Radioligand
Conc. (nM) Kd (nM)
5HT1A HEK293 3H-8-0H-DPAT 0.5
0.557
5HT2A NIH3T3 3H-ketanserin 2
0.628
5HT2B CHO 3H-5-HT 4
2.312
5HT2c CHO 3H-mesulergin 1
1.909
5HT3A/B HEK293 3H-GR65630 0.5
0.247
5HT4B HEK293 3H-GR113808 0.1
0.059
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Receptor Cell line Radioligand Conc. (nM) Kd (nM)
Alpha' A CHO 3H-prazosin 0.25 0.226
Alpha2A CHO 3H-rauwolscine 1 0.485
Alpham CHO 3H-rauwolscine 1 0.853
Alpha2c CHO 3H-rauwolscine 1 0.100
D2L CHO 3H-spiperone 0.2 0.239
hERG HEK293 3H-dofetilide 5 3.66
The % inhibition of binding of the radioligand to the receptor induced by the
test
compound was calculated by the formula %Effect = 100-[(sample-NSB) / (HC-NSB)
*
100], where sample = radioactive count in a drug treated well, HC =
radioactive count
in control wells incubated with radioligand only. Using in house developed
software, a
best-fit curve was fitted by a minimum sum of squares method to the plot of %
inhibition vs. concentration of the test compound. From this, the pIC50 value
(inhibitory concentration causing 50 % displacement of specific binding) was
determined, as well as an estimate of the slope of the plot (Hill
coefficient).
Table 2 : pIC50 values
Co.No. Ref ( )-17 (+)-17 (-)-17 ( )-7 (+)-7 (-)-7 ( )-12 (+)-12 (-)-12
trend
Target
5HT1A 5.71 5.1 5.25 <5 5.74 6.17 5.96 5.38 6.13 5.73 =
5HT2A 7.84 5.71 5.59 5.76 6.95 7.15 6.12 6.44 6.49 6.31 4/
5HT2B 6.62 7.86 7.29 8.14 6.97 6.89 6.6 7.18 6.83 7.14 t
5EIT2c 5.73 5.33 <5 5.18 5.74 5.91 5.43 5.36 5.3 5.18 =
5HT3A/B 5.94 <5 <5 <5 <5 <5 <5 5.17 <5 5.56
5HT4B 6.65 <5 <5 <5 6.21 6.06 6.36 6.94 6.9 6.27
AlphaiA 6.39 <5 <5 5.11 <5 6.28 6.4 6.35 6.26 6.48
Alpha2A 6.05 <5 <5 <5 5.44 <5 5.11 5.32 5 5.09
Alpham 6.19 <5 <5 <5 5.6 5.58 5.22 5.6 5.47 5.28
Alpha2c 6 <5 <5 <5 6.02 <5 5.93 5.68 5.71 5.23
D2L 6.27 4.98 <5 <5 5.34 5.56 5.10 5.33 5.32 5.32 4/
hERG 7.42 5.12 <5 <5 6.63 6.54 6.5 6.5 6.75 6.72 4/
The reference compound (Ref) is cisapride.
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Example 5 : 5-HT 2B antagonism
CHO-K 1 (ECACC) cells were stably transfected with human 5-HT2B receptor cDNA
subcloned into pCDNA3.1 using the calcium phosphate method. Stably transfected
cell
lines were selected using G-418, and clonal cell lines were developed by limit
dilution.
Cell lines were cultured in Dulbecco's modified Eagle Medium (DMEM) containing
10% heat inactivated dialyzed foetal bovine serum (FBS), 1% penicillin-
streptomycin,
1% L-glutamine and 1% non-essential amino acids.
Confluent monolayers plated into black 96 well plates with clear bottoms were
loaded
with 4 uM Fluo-3-AM for 90 min at 37 C in Hanks balanced salt solution
supplemented with 20 mM HEPES and 2.5 mM probenecid. After washing, the test
compound was added to the cells and maximal fluorescence in response to 0.1 nM
serotonin was recorded using a fluorometric imaging plate reader (FLIPR) to
detect
changes in intracellular calcium levels.
The maximal fluorescence recorded in the presence of the test compound was
expressed as a percent of the maximal fluorescence response to the agonist
serotonin
(0.1 nM). The IC50 value was determined by non-linear regression analysis of
the
concentration-response curves generated with mean replicate values using Hill
equation
curve fitting (Y = D + [(A ¨ D)/(1 + (C/C50)nH)], where Y = specific response,
D =
minimum specific response (no drugs or serotonin added), A = maximum specific
response (0.1 nM serotonin, no drugs), C = concentration of compound, and C50
= IC50,
and nil = slope factor) (SigmaPlot 4.0, SPSS Inc.). The apparent dissociation
constant (KB) was calculated using the modified Cheng Prusoff equation (KB =
IC50/(1+(A/EC50A)), where A = concentration of serotonin, and EC50A = EC50
value of
serotonin in this assay). (Porter et al. (1999), Br. J. Pharmacol., 128: 13-
20)
Table 3 : 5-HT2B antagonism
Compound IC50 KB
( )-7 60 nM 20 nM
0-12 12 nM 4.2 nM
(+)-17 33 nM 11 nM
(-)-17 1.6 nM 0.55 nM
Example 6 : hERG-transfected HEK293 cells using a Patch Express apparatus.
Experiments were performed using HEK293 cells stably expressing the hERG
potassium channel. Cells were grown at 37 C and 5% CO2 in culture flasks in
MEM
Medium supplemented with 10% heat-inactivated fetal bovine serum, 1% L-
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Glutamine-Penicillin-Streptomycin-solution, 1% non-essential amino acids
(100x), 1%
sodium pyruvate (100mM) and 0.8% Geneticin (50mg/m1). Before use the cells
were
subcultured in MEM medium in the absence of 5 ml L-Glutamine-Penicillin-
Streptomycin. For use in the automated patch-clamp system PatchXpress 7000A
(Axon
Instruments) cells were harvested to obtain cell suspension of single cells.
Extracellular solution contained (mM): 150 NaC1, 4 KC1, 1 MgC12, 1.8 CaC12, 10
HEPES, 5 Glucose (pH 7.4 with NaOH). Pipette solution contained (mM): 120 KC1,
10
HEPES, 5 EGTA, 4 ATP-Mg2, 2 MgC12, 0.5 CaC12 (pH 7.2 with KOH).
Patch-clamp experiments were performed in the voltage-clamp mode and whole-
cell
currents were recorded with an automated patch-clamp assay utilizing the
PatchXpress
7000A system (Axon Instruments). Current signals were amplified and digitized
by a
Multiclamp amplifier, stored and analyzed by using the PatchXpress, DataXpress
software and Igor 5.0 (Wavemetrics).
The holding potential was -80 mV. The hERG current (K+-selective outward
current)
was determined as the maximal tail current at -40 mV after a 2 second
depolarization to
+60 mV. Pulse cycling rate was 15 s. Before each test pulse a short pulse (0.5
s) from
the holding potential to -60 mV was given to determine (linear) leak current.
After establishing whole-cell configuration and a stability period, the
vehicle (aqueous
DMSO control) was applied for 5 minutes followed by the test substance by
increasing
concentrations of 10-7 M, 3 x 10-7 M and 3 x 10-6 M.
Each concentration of the test substance was applied twice. The effect of each
concentration was determined after 5 min as an average current of 3 sequential
voltage
pulses. To determine the extent of block the residual current was compared
with
vehicle pre-treatment. Data are expressed as % block at the indicated
concentrations in
Table 4. The values between brackets refer to % block by the vehicle.
Table 4 : % block of the hERG channel
Concentration 100 nM 300 nM 3000 nM
Cisapride 80(7) 95 (15) not tested
( )-7 35 (7) 62 (15) 94 (21)
0-12 40 (7) 73 (15) 96 (21)
0-17 9(7) 17(15) 58(21)
(+)-17 14(7) 21(10) 52(11)
(-)-17 3(7) 11(10) 47(11)
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Example 7: Monocrotaline-induced pulmonary arterial hypertension in the rat
Compound (-)-17 was tested in monocrotaline-induced pulmonary arterial
hypertension
in the rat (see e.g., Stenmark et al, 2009, Am J Physiol Lung Cell Mol Physiol
297,
L1013¨L1032). Measurements included: mean arterial blood pressure and right
ventricular pressure in vivo, ratio of right ventricular weight to left
ventricular weight
plus septum as an index of right ventricular hypertrophy, pulmonary artery
acceleration
time, and histological assessement of muscularization of pulmonary arteries.
Monocrotaline was dissolved in 1 N HC1 and then into distilled water, and pH
was
adjusted to 7.4 using NaOH. A single dose of 60 mg/kg monocrotaline was
administered subcutaneously on day 0 to three groups of male Sprague Dawley
rats.
The test article Compound (-)-17 was dissolved in 20% hydroxypropyl-beta-
cyclodextrin with NaOH, HC1 and mannitol in pyrogen-free water and
administered
orally by gavage (10 ml/kg) once daily from day 1 for 21 days at 10 mg/kg and
50
mg/kg. Plasma concentrations of Compound (-)-17 were measured 2 hours
(approximate Cmax after oral dosing in rats) after the final administration on
day 21.
Corresponding volumes of 20% hydroxypropyl-beta-cyclodextrin vehicle were
administered orally according to the same protocol in a third group of
animals.
Three-week treatments with Compound (-)-17 at 10 mg p.o. once daily (mean
plasma
concentration 2 hours post-dosing at day 21 ¨80 ng/ml) and at 50 mg p.o. once
daily
(mean plasma concentration ¨1,000 ng/ml) were non-toxic, and had no effect on
mean
arterial blood pressure (MAP), but reduced right ventricular pressure (RVP),
right
ventricular hypertrophy (right ventricle/(left ventricle + septum);
RV/(LV+S)), and
increased pulmonary artery acceleration time (PAAT) (Table 5). The mean wall
thickness of small pulmonary arteries was significantly increased by
monocrotaline
treatment, and this thickening was reduced by a three-week treatment with
Compound
(-)-17 at 50 mg/kg p.o. (P=0.0539) and at 10 mg p.o. (P<0.005).
Table 5:
Treatment MAP (mmHg) RVP (mmHg) RV/(LV+S) PAAT (ms)
Vehicle 92.53 20.18 52.45 9.16 0.66 0.16 11.63 2.36
Compound(-)-17 93.7 14.11 43.18 7.38 * 0.46 0.08 * 15.91 2.76
*
10 mg/kg p.o.
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Treatment MAP (mmHg) RVP (mmHg) RV/(LV+S)
PAAT (ms)
Compound(-)-17 97.58 9.74 42.85 11.55 * 0.41 0.08 *
15.42 2.62 *
50 mg/kg p.o.
Values are mean SD measured at Day 21. * p <0.05 compared to vehicle
Example 8: Cardiovascular effects in the anaesthetized guinea-pig
Female guinea-pigs were anesthetized with sodium pentobarbital (66 mg/kg i.p.)
followed by a continuous i.v. infusion of 6 mg/h of sodium pentobarbital and
prepared
for measurements of the surface electrocardiogram (ECG), heart rate and mean
arterial
blood pressure (see De Clerck et al, Fundam. Clin. Pharm.; 2002; 16: 125-140).
Compound (-)-17 was dissolved in 20% hydroxypropyl-cyclodextrin with NaOH, HC1
and mannitol in pyrogen-free water and administered intravenously (0.5m1/kg)
in
increasing doses (0.16, 0.32, 0.64, 1.25, 2.5 and 5 mg/kg) over a period of 5
min at 15-
min intervals. Plasma concentrations of Compound (-)-17 were measured at the
end of
each infusion. Corresponding volumes of vehicle were administered according to
the
same protocol in a second group of animals.
Relative to vehicle, Compound (-)-17 at 0.16 up to 5 mg/kg (total dose: 9.87
mg/kg;
Cmax: 11,950 ng/ml) had no relevant effect on heart rate, the duration of the
PQ, QRS,
QT and QTcB intervals, or on ECG morphology in the anesthetized guinea-pig
(Table
6). From 2.5 mg/kg onwards (Cmax: 6,325 ng/ml; Table 7), mean arterial blood
pressure started to increase (Table 6).
The reference compound dofetilide (0.02 mg/kg i.v. over 1 min), given 15 min
after the
onset of the last infusion of vehicle, decreased heart rate and prolonged the
QT and
QTcB intervals.
Table 6: Effects of Compound (-)-17 before and at 2, 5 and 15 minutes after
onset of
each infusion, expressed as percentage changes relative to baseline values on
heart rate
(HR), mean arterial blood pressure (MBP) and on ECG parameters in anesthesized
guinea pigs. Baseline values are presented as actual units.
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Parameter HR b/min MBP PQ ms QRS ms QT ms QTc B ms
mmHg
Baseline 230 33 63 31 185 361
0.16 mg/kg @ 2' -1% 4% 0% -2% 0% -1%
0.16 mg/kg @ 5' 0% 13% 1% -2% -1% -1%
0.16 mg/kg @ 15' -2% -3% 4% 0% 1% 1%
0.32 mg/kg @ 2' -1% 6% 2% -2% 0% 1%
0.32 mg/kg @ 5' -4% 2% 4% 0% 3% 1%
0.32 mg/kg @ 15' -4% -3% 4% 0% 4% 3%
0.64 mg/kg @ 2' -5% 6% 5% 0% 7% 4%
0.64 mg/kg @ 5' -2% 13% 5% -5% 5% 2%
0.64 mg/kg @ 15' -5% -5% 4% -3% 8% 4%
1.25 mg/kg @ 2' -7% 4% 5% -2% 8% 4%
1.25 mg/kg @ 5' -7% 15% 6% 0% 6% 2%
1.25 mg/kg @ 15' 0% 9% 6% -3% 2% 3%
2.5 mg/kg @ 2' -5% 17% 7% -3% 6% 4%
2.5 mg/kg @ 5' -6% 21% 7% -3% 6% 3%
2.5 mg/kg @ 15' -4% 8% 8% 0% 6% 5%
mg/kg @ 2' -3% 36% 6% -2% 7% 5%
5 mg/kg @ 5' -3% 34% 6% 0% 3% 2%
Values are median of n=6. Statistically significant differences (p < 0.05) are
indicated
in bold and italic, and were calculated on the changes from baseline in actual
units.
Table 7: Median plasma levels of Compound (-)-17 (ng/ml) after administration
of
5 increasing intravenous doses of 0.16, 0.32, 0.64, 1.25, 2.5 and 5 mg/kg
over periods of
5 minutes at 15-minute intervals (n=6)
Dose 0.16 0.32 0.64 1.25 2.5 5
Median 398 873 1815 3330 6325 11950
Example 9: Bleomycin-induced lung fibrosis in the mouse (prophetic)
Male C57BL/6 mice are treated intratracheally with bleomycin sulfate (aqueous
solution 2.5 U/ml; 2 ml/kg BW) under isoflurane inhalation anesthesia (see
e.g., Ishii Y
et al, 2006. Am J Respir Crit Care Med. 174(5):550-6). Thereafter Compound (-)-
17 is
administered once daily for 2 weeks at 10 mg/kg and 50 mg/kg p.o. Post-mortem
examination includes gross pathology, lung weights and lung histopathology on
Day
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15. Histopathological examination of the lungs indicates that bleomycin causes
inflammation followed by fibrosis in the lungs in untreated mice.
Example 10: Pharmacokinetic evaluation in the mouse
For intravenous (i.v.) administration, Compound (-)-17 was dissolved in saline
containing 20% (w/v) hydroxy-propyl-beta-cyclodextrin (HPbCD) at a
concentration of
0.25 mg/mL and administered (10 mL/kg) to male CD1 mice (n =3) as a bolus via
a tail
vein at a dose level of 2.5 mg/kg. For oral (p.o.) administration, Compound (-
)-17 was
dissolved in water containing 20% (w/v) HPbCD at a concentration of 0.5 mg/mL
and
administered (20 mL/kg) to male CD1 mice (n =3) via gavage at a dose level of
10
mg/kg. Blood samples were collected via a saphenous vein at serial time points
up to
24 h after dosing. Plasma was obtained by centrifugation and stored at -20 C
prior to
analysis. Analysis was performed using liquid chromatography (LC) with tandem
mass
spectrometric detection (MS/MS) in positive ion mode. Compound (-)-17 was
eluted
from a reversed phase column with a gradient of acetonitrile and water
containing 0.1%
(v/v) formic acid. At the time of analysis plasma samples (20 uL) were thawed
and
deprotonated with 200 uL of acetonitrile and centrifuged. Aliquots of the
supernatant
were injected onto a reversed phase UPLC column and analysed via electrospray
Mass
Spectrometry. Calibration standards and quality controls, analysed before and
after the
study samples, were prepared in mouse plasma at the same time as the. The
accuracy
(intra branch accuracy from independent QC samples) was between 85 % and 115 %
of
the nominal value over the entire concentration range. Non-compartmental
pharmacokinetic analysis of the plasma concentration-time curves was performed
using
WinNonLin to provide estimates of the plasma clearance (CLp), volume of
distribution
at steady-state (Vss), terminal phase elimination half-life (t1/2) and oral
bioavailability
(F), the results are summarised in Table 8.
Example 11: Pharmacokinetic evaluation in the rat
For intravenous (i.v.) administration, Compound (-)-17 was dissolved in saline
containing 20% (w/v) hydroxy-propyl-beta-cyclodextrin (HPbCD) at a
concentration of
1 mg/mL and administered (2.5 mL/kg) to male Sprague Dawley rats (n =1) as a
bolus
via a saphenous vein at a dose level of 2.5 mg/kg. For oral (p.o.)
administration,
Compound (-)-17 was dissolved in water containing 20% (w/v) HPbCD at a
concentration of 1 mg/mL and administered (10 mL/kg) to male Sprague Dawley
rats
(n = 3) via gavage at a dose level of 10 mg/kg. Blood samples were collected
via a tail
vein at serial time points up to 24 h after dosing. Plasma was obtained by
centrifugation
and stored at -20 C prior to analysis. Analysis was performed using liquid
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chromatography (LC) with tandem mass spectrometric detection (MS/MS) in
positive
ion mode. Compound (-)-17 was eluted from a reversed phase column with a
gradient
of acetonitrile and water containing 0.1% (v/v) formic acid. At the time of
analysis
plasma samples (50 uL) were thawed and deprotonated with at least three
volumes of
acetonitrile and centrifuged. Aliquots of the supernatant were injected onto a
reversed
phase UPLC column and analysed via electrospray Mass Spectrometry. Calibration
standards and quality controls, analysed before and after the samples, were
prepared in
rat plasma at the same time as the study samples. The accuracy (intra branch
accuracy
from independent QC samples) was between 85% and 115% of the nominal value
over
the entire concentration range. Non-compartmental pharmacokinetic analysis of
the
plasma concentration-time curves was performed using WinNonLin to provide
estimates of the plasma clearance (CLp), volume of distribution at steady-
state (Vss),
terminal phase elimination half-life (t1/2) and oral bioavailability (F), the
results are
summarised in Table 8.
Table 8: Non-Compartmental Pharmacokinetic Parameters for Compound (-)-17
obtained in Mouse and Rat Following i.v. and p.o. Administration of Compound (-
)-17-
AAA (the free base).
Parameter Mouse Rat
CL (mL/min/kg) 20 6 46
Vss (L/kg) 1.9 0.6 3.1
t1/2 (h) 1.4 0.2 1.1
Cmax (ng/mL) PO 1580 165 119 37
Tmax (h) PO 0.5 [0.5-1.0] 0.5
AUC(0-t) (ng.h/mL) PO 4443 1093 686 254
F(%) 52 19
Example 12: Cardio-hemodynamic, cardio-electrophysiological,
electroencephalographic and pulmonary/respiratory effects in artificially
ventilated,
anesthetized dogs (Beagles)
The animals were anesthetized with a mixture of 0.015 mg/kg i.v. scopolamine
and
0.075 mg/kg i.v. lofentanil, and relaxed with succinylcholine (5 mg/kg i.v.)
followed by
a continuous i.v. infusion of 1.5 mg/kg/h of etomidate and small additional
doses of
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fentanyl (0.025 mg/kg i.v.) were given at 60 min intervals. The animals were
ventilated
and prepared for measurements of the surface ECG, aortic-, pulmonary- and left
ventricular blood pressure, carotid blood flow, monophasic action potential,
body
temperature, blood gasses and EEG (see Van Deuren et al, J Pharmacol Toxicol
Methods; 2009; 60: 11-23). Compound (-)-17 was dissolved in 20% hydroxypropyl-
cyclodextrin with NaOH, HC1 and mannitol in pyrogen-free water and
administered
intravenously (1 ml/kg) in increasing doses (0.16, 0.32, 0.63, 1.25, 2.5 and 5
mg/kg)
over a period of 5 min at 30-min intervals. Plasma concentrations of Compound
(-)-17
were measured before and at the end of each infusion. Corresponding volumes of
vehicle were administered according to the same protocol in a second group of
animals.
Relative to vehicle, Compound (-)-17 at 0.16 up to 5 mg/kg (total dose: 9.86
mg/kg;
median Cmax: 20,375 ng/ml) had no relevant effect on heart rate (HR),
pulmonary
artery pressure, left ventricular end diastolic pressure, cardiac output,
stroke volume,
pressure rate product, the duration of the PQ and QRS intervals, lung function
(dynamic compliance, Cdyfl and airway resistance, Raw), body temperature or on
EEG
(measured by the Narcotrendg) in the anesthetized dog. From 1.25 mg/kg onwards
(Cmax: 5,205 ng/ml), arterial blood pressure, vascular resistance (systemic
and
common carotid) and Tau (time constant of relaxation) started to increase.
Furthermore, at 2.5 mg/kg (Cmax: 9,550 ng/ml) LV dp/dtmax/pd started to
decrease and
at 5 mg/kg (Cmax: 20,375 ng/ml) a minor decrease was noted in the duration of
QTc
VDW (QT interval corrected for FIR) and QTc VcT (QT interval corrected for HR
and
temperature).
Table 9: Effects of Compound (-)-17 before and at 5 and 30 minutes after onset
of each
infusion, expressed as percentage changes relative to vehicle, on heart rate
(HR), mean
arterial blood pressure (MBP), systolic (SPP) and diastolic (DPP) pulmonary
pressure,
left ventricular contractility (LVdpidtmax ) and ECG parameters (PQ, QRS and
QTcV) in
anesthetized beagle dogs. Baseline values are presented as actual units.
Parameters HR MBP SPP DPP
LVdp/dt. PQ ms QRS QTcV
Units b/min mmHg mmHg mmHg mmHg/s
ms ms
Baseline 64 103 29 12
3123 97 46 294
0.16 mg/kg @ 5' -4% +2% +2% +3%
-1% -1% +1% +2%
0.16 mg/kg @ 30' -5% +3% +5% -3%
+0% -0% +2% +4%
0.32 mg/kg @ 5' -5% +5% +11% +0%
+0% -2% +3% +2%
0.32 mg/kg @ 30' +3% +2% -3% -8%
-4% -2% +4% +1%
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- 31 -
Parameters HR MBP SPP DPP LVdp/dt. PQ ms QRS QTcV
Units b/min mmHg mmHg mmHg mmHg/s ms
ms
Baseline 64 103 29 12 3123 97 46
294
0.63 mg/kg @ 5' -0% +6% -2% +0% -3% +3% +4%
+1%
0.63 mg/kg @ 30' +4% +2% -1% -9% -2% -0% +1%
+4%
1.25 mg/kg @ 5' -0% +10% -1% -7% -1% +2% +4%
+2%
1.25 mg/kg @ 30' -3% +0% -9% -12% -5% +2% +2%
+1%
2.5 mg/kg @ 5' -5% +13% -1% +1% -8% +6% +2% -
3%
2.5 mg/kg @ 30' -4% +0% -15% -24% +2% +2% +3% -
1%
mg/kg @ 5' -15% +17% -10% +17% -11% +2% +6% -3%
5 mg/kg @ 30' -14% +0% -7% -5% +2% +-2% +3% -
2%
Values are median of n = 4. Statistically significant differences (p < 0.05)
are indicated
in bold and italic, and were calculated on the changes from baseline in actual
units.
Table 10: Median plasma levels of Compound (-)-17 (ng/ml) after administration
of
5 increasing intravenous doses of 0.16, 0.32, 0.64, 1.25, 2.5 and 5 mg/kg
over periods of
5 minutes at 30-minute intervals (n=4).
Dose (mg/kg) 0.16 0.32 0.64 1.25 2.5 5
Median (ng/ml) 725 1420 2540 5205 9550 20375